Confinement of pyridinium hemicyanine dye within an anionic metal-organic framework for two-photon-pumped lasing

被引:401
|
作者
Yu, Jiancan [1 ]
Cui, Yuanjing [1 ]
Xu, Hui [1 ]
Yang, Yu [1 ]
Wang, Zhiyu [1 ]
Chen, Banglin [1 ,2 ]
Qian, Guodong [1 ]
机构
[1] Zhejiang Univ, Dept Mat Sci & Engn, State Key Lab Silicon Mat, Cyrus Tang Ctr Sensor Mat & Applicat, Hangzhou 310027, Peoples R China
[2] Univ Texas San Antonio, Dept Chem, San Antonio, TX 78249 USA
来源
NATURE COMMUNICATIONS | 2013年 / 4卷
基金
中国国家自然科学基金;
关键词
AMPLIFIED SPONTANEOUS EMISSION; MICROPOROUS METAL; FLUORESCENCE; CRYSTAL; RECOGNITION; TRANSPORT; PORES; SITES;
D O I
10.1038/ncomms3719
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Two-photon-pumped dye lasers are very important because of their applications in wavelength up-conversion, optical data storage, biological imaging and photodynamic therapy. Such lasers are very difficult to realize in the solid state because of the aggregation-caused quenching. Here we demonstrate a new two-photon-pumped micro-laser by encapsulating the cationic pyridinium hemicyanine dye into an anionic metal-organic framework (MOF). The resultant MOF superset of dye composite exhibits significant two-photon fluorescence because of the large absorption cross-section and the encapsulation-enhanced luminescent efficiency of the dye. Furthermore, the well-faceted MOF crystal serves as a natural Fabry-Perot resonance cavity, leading to lasing around 640 nm when pumped with a 1064-nm pulse laser. This strategy not only combines the crystalline benefit of MOFs and luminescent behaviour of organic dyes but also creates a new synergistic two-photon-pumped lasing functionality, opening a new avenue for the future creation of solid-state photonic materials and devices.
引用
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页数:7
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